List of variants reported as likely pathogenic for primary adrenal insufficiency by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.850A>G (p.Met284Val)	rs770199817	0.00007
NM_006440.5(TXNRD2):c.1321C>T (p.Arg441Ter)	rs200162480	0.00002
NM_000500.9(CYP21A2):c.710T>A (p.Ile237Asn)	rs1554299737	0.00001
NM_000500.9(CYP21A2):c.713T>A (p.Val238Glu)	rs12530380	0.00001
NM_000102.4(CYP17A1):c.987C>G (p.Tyr329Ter)
NM_000500.9(CYP21A2):c.1066C>T (p.Leu356=)	rs1776234662
NM_000500.9(CYP21A2):c.1131C>G (p.Tyr377Ter)
NM_000500.9(CYP21A2):c.293-13C>G	rs6467
NM_000500.9(CYP21A2):c.68G>A (p.Trp23Ter)
NM_000500.9(CYP21A2):c.710_719del (p.Ile237fs)
NM_000500.9(CYP21A2):c.844G>T (p.Val282Leu)	rs6471

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